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Cytomegalovirus, DNA by PCR, Quantitative (Viral Load)
Test CodeCMVAL
Alias/See Also
CMV
CPT Codes
87497
Includes
- IU/mL
- Log (IU/mL)
Preferred Specimen
2 mL Plasma collected in EDTA (lavender top) tube
Minimum Volume
0.900 mL Plasma
Note: minimum volume does not allow for repeat testing
Note: minimum volume does not allow for repeat testing
Other Acceptable Specimens
Plasma collected in EDTA gel separator (pearl top) EDTA
Instructions
Centrifuge for complete separation of plasma and red cells. Aliquot (transfer) plasma into a standard transport tube. Refrigerate until tested.
Transport Container
Standard transport tube
Transport Temperature
Refrigerated
Specimen Stability
2-8°C for 5 days, Whole Blood or Plasma
-20°C, Frozen, Plasma
-20°C, Frozen, Plasma
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
The following conditions will result in sample rejection:
- Quantity not sufficient
- Samples collected in any heparin tube
Methodology
PCR (Polymerase Chain Reaction)
FDA Status
Approved
Setup Schedule
Monday & Thursday only
Report Available
Report available within 24 hours after testing.
Limitations
Due to the potential for variability in CMV viral load measurements across different CMV assays, it is recommended that the same device be used for the quantitation of CMV viral load when managing CMV infection in individual patients.
Reference Range
30 - 100,000,000 IU/mL or 1.48 - 8.00 log (IU/mL)
Clinical Significance
This assay is intended for use as an aid in the management of solid organ transplant and hematopoietic stem cell transplant (HSCT) patients who have been diagnosed with CMV disease and are undergoing antiviral therapy.
Performed By
Alverno Laboratories
Performing Laboratory
Alverno Central Lab
NIMAM (Alinity m)
Last Updated: April 30, 2026

